Clinical Research Patient Care

PRAGYNA MADOORI

816-***-****

ad12qx@r.postjobfree.com

CLINICAL RESEARCH ASSISTANT

PROFESSIONAL EXPERIENCE:

Have acquired approximately six years of extensive experience in the field of clinical research and healthcare.

Possess excellent analytical and planning capabilities, demonstrating a strong commitment to achieving objectives within designated timelines.

Experienced in conducting Electronic Data Capture (EDC) trials.

Collaborated with the principal investigator, Clinical Research Coordinator, and sponsors to effectively manage daily trial activities and ensure adherence to research protocols.

Ensured adherence to protocols governing patient care and operations for clinical trials. Facilitated proper shipping, handling, and storage of Investigational Medical Products.

Clinical trials focused on disorders such as Ulcerative colitis were efficiently coordinated.

Identified and Reported AE and SAE.

Assessed lab reports by screening patient records.

Have had the opportunity to participate in site initiation visits and investigator meetings.

Maintained thorough records and diligently followed up with informed consent.

Collected data and research protocols were followed, adhering to operations manuals as well as meeting case report form requirements.

Scheduled, conducted, and documented study visits.

Adhered to the principles of Good Clinical Practice.

Ensure the collection of high-quality and valid data by adhering to the ALCOA-C principle.

Achieved knowledge about FDA regulations 21 CFR 11,50,54,56.

PROFESSIONAL EXPERIENCE

Role: CRC AIG Hospitals (June 2019 -February 2021)

Responsibilities:

·Worked as a CRC at AIG hospitals and worked on Ulcerative colitis study

·Identified and screened potential patients for the Study, and explained the study requirements and obtained Informed Consent

·Organized and scheduled study visits, laboratory procedures for participants.

·Collection and recording of data from Study participants, including medical history, vital signs, study specific measurements.

·Ensuring the data quality and integrity are met.

·AE and SAE reporting promptly

·Worked closely with PI, SI, and other team members of the study team.

·Adhering to Good Clinical Practice guidelines and relevant regulations.

·Maintaining and organizing the study files CRF and other study related documents.

·Participated in site initiation visits.

Role: Apollo Hospitals (January 2014 - May 2019)

Responsibilities:

·Worked as a Medical Doctor for 5+ years.

·Dedicated and compassionate doctor with good experience in outpatient care, OB/GYN.

·Skilled in providing comprehensive patient care, diagnosing, and treating medical conditions, and collaborating with interdisciplinary healthcare teams.

·Strong communication and interpersonal skills with a patient-centered approach.

·Diagnosing, treating, and managing the medical conditions.

·Proficiency in Medical terminologies.

·Providing medical advice and Consultation to patients.

Certifications:

Good clinical practice Certificate by NIH (NIDA Clinical Trial Networks).

EDUCATION

Bachelor of Medicine, Bachelor of Surgery (MBBS/MD) from Chongqing Medical University

SKILLS

●MS Office – Excel, Word, PowerPoint, MS Project

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